Duns Number:002065670
Device Description: Tubing, Replacement, 100cm (39in) LuerF x LuerM Extension. Used on 00-197, (10) Tubing se Tubing, Replacement, 100cm (39in) LuerF x LuerM Extension. Used on 00-197, (10) Tubing sets
Catalog Number
00-197-TUBING
Brand Name
AincA®
Version/Model Number
00-197-TUBING
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
MRI safety Status
MR Safe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K912723,K912723
Product Code
BSK
Product Code Name
Cuff, tracheal tube, inflatable
Public Device Record Key
1e3f698b-8d72-4daf-83cf-af8b1bd33c24
Public Version Date
April 08, 2021
Public Version Number
1
DI Record Publish Date
March 31, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 561 |
2 | A medical device with a moderate to high risk that requires special controls. | 135 |